state board — 3 things I got wrong before I got it right
The title is the argument: state board — 3 things I got wrong before I got it right. Here is the rest of it. Nothing in this thread is medical advice, and the choice between arrangements is one for you and a prescriber who knows your history. Potency and sterility testing on the finished preparation are separate from…
salt forms are the recurring argument and the answer is boring
salt forms are the recurring argument and the answer is boring
Adding one thing — ask for the facility name. Most will give it, and the ones that will not have answered you.
Right, and the concentration genuinely can differ from the branded product, which breaks people’s arithmetic.
A beyond-use date derived from published stability data means something different from one assigned by default rule. Asking which is a fair question and the answer is usually available.
Yes. The shortage list is the legal hinge for the whole arrangement and its status is public.
potency testing on the finished preparation is the thing to ask for
the label on a compounded vial is a legal document, read it
the label on a compounded vial is a legal document, read it
Disagreeing with this bit: registration is not equivalence, and the two get run together constantly.
This. Compounded preparations carry no equivalence claim, and treating them as generics is a category error people make constantly.